CSIR - Centre for Cellular & Molecular Biology
Council of Scientific and Industrial Research
The Innovation Engine of India
Reconstructing the demographic history of the Himalayan and adjoining populations
Hum Genet. 137:129-139.
Author Response: Penetrance of the LHON Mutation m.11778G>A May Depend on Factors Other Than Haplotype or Heteroplasmy Rate
Invest Ophthalmol Vis Sci. 59:382
Outcome of epilepsy in patients with mitochondrial disorders: Phenotype genotype and magnetic resonance imaging correlations
Clin Neurol Neurosurg. 164:182-189
NR5A1 mutations are not associated with male infertility in Indian men
Andrologia 50: e12931
Vitamin B(12) supplementation influences methylation of genes associated with Type 2 diabetes and its intermediate traits
Epigenomics. 2018 Jan;10(1):71-90. doi: 10.2217/epi-2017-0102. Epub 2017 Nov 14.
Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls
Sci Data. 2018 Jan 23;5:180002. doi: 10.1038/sdata.2018.2.
Identification and characterization of cis-regulatory elements \'insulator and repressor\' in PPARD gene
Epigenomics. 2018 May;10(5):613-627. doi: 10.2217/epi-2017-0139. Epub 2018 Mar 27.
Candidate genes linking maternal nutrient exposure to offspring health via DNA methylation: a review of existing evidence in humans with specific focus on one-carbon metabolism
Int J Epidemiol. 2018 Dec 1;47(6):1910-1937. doi: 10.1093/ije/dyy153.
Adult onset hereditary hemochromatosis is associated with a novel recurrent Hemojuvelin (HJV) gene mutation in north Indians
Blood Cells Mol Dis. 2018 Nov;73:14-21. doi: 10.1016/j.bcmd.2018.08.003. Epub 2018 Aug 27.
DNA Techniques in Wildlife Forensics (Animals): Standard Operating Procedures (SOP)
A SOP